ES2139754T3 - 3-PHENYL-2-ISOXAZOLINES AS ANTI-INFLAMMATORY AGENTS. - Google Patents

3-PHENYL-2-ISOXAZOLINES AS ANTI-INFLAMMATORY AGENTS.

Info

Publication number
ES2139754T3
ES2139754T3 ES94927778T ES94927778T ES2139754T3 ES 2139754 T3 ES2139754 T3 ES 2139754T3 ES 94927778 T ES94927778 T ES 94927778T ES 94927778 T ES94927778 T ES 94927778T ES 2139754 T3 ES2139754 T3 ES 2139754T3
Authority
ES
Spain
Prior art keywords
isoxazolines
phenyl
inflammatory agents
dermatitis
aryl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
ES94927778T
Other languages
Spanish (es)
Inventor
Edward F Kleinman
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pfizer Corp Belgium
Pfizer Corp SRL
Original Assignee
Pfizer Corp Belgium
Pfizer Corp SRL
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pfizer Corp Belgium, Pfizer Corp SRL filed Critical Pfizer Corp Belgium
Application granted granted Critical
Publication of ES2139754T3 publication Critical patent/ES2139754T3/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D261/00Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/04Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6527Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07F9/653Five-membered rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Molecular Biology (AREA)
  • Virology (AREA)
  • Pulmonology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Biochemistry (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Immunology (AREA)
  • Dermatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

ESTA INVENCION SE REFIERE A COMPUESTOS DE 3-ARIL-2ISOXAZOLINAS QUE SON INHIBIDORES SELECTIVOS DE FOSFODIESTERASA TIPO IV (FFDIV). LAS 3-ARIL-2-ISOXAZOLINAS SON UTILES EN EL TRATAMIENTO DE SIDA, ASMA, ARTRITIS, BRONQUITIS, ENFERMEDADES CRONICAS DE OBSTRUCCION PULMONAR, PSORIASIS, RINITIS ALERGICA, DERMATITIS, SHOCK, DERMATITIS ATOPICA, ARTRITIS REUMATOIDE Y OSTEOARTRITIS. ESTA INVENCION TAMBIEN SE REFIERE A COMPOSICIONES FARMACEUTICAS UTILES PARA LO MISMO.THIS INVENTION REFERS TO 3-ARYL-2ISOXAZOLINE COMPOUNDS WHICH ARE SELECTIVE INHIBITORS OF TYPE IV PHOSPHODIESTERASE (FFDIV). 3-ARYL-2-ISOXAZOLINS ARE USEFUL IN THE TREATMENT OF AIDS, ASTHMA, ARTHRITIS, BRONCHITIS, CHRONIC DISEASES OF PULMONARY OBSTRUCTION, PSORIASIS, ALLERGIC RHINITIS, DERMATITIS, SHOCK, ATOPICA DERMATITIS, RHEUMARI AND OSTRUM THIS INVENTION ALSO REFERS TO USEFUL PHARMACEUTICAL COMPOSITIONS FOR THE SAME.

ES94927778T 1993-11-26 1994-10-12 3-PHENYL-2-ISOXAZOLINES AS ANTI-INFLAMMATORY AGENTS. Expired - Lifetime ES2139754T3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US15724193A 1993-11-26 1993-11-26

Publications (1)

Publication Number Publication Date
ES2139754T3 true ES2139754T3 (en) 2000-02-16

Family

ID=22562909

Family Applications (1)

Application Number Title Priority Date Filing Date
ES94927778T Expired - Lifetime ES2139754T3 (en) 1993-11-26 1994-10-12 3-PHENYL-2-ISOXAZOLINES AS ANTI-INFLAMMATORY AGENTS.

Country Status (12)

Country Link
US (1) US5686434A (en)
EP (1) EP0730587B1 (en)
JP (1) JP2818820B2 (en)
AT (1) ATE187447T1 (en)
CA (1) CA2177375A1 (en)
DE (1) DE69422061T2 (en)
DK (1) DK0730587T3 (en)
ES (1) ES2139754T3 (en)
FI (1) FI945556A7 (en)
GR (1) GR3032506T3 (en)
PT (1) PT730587E (en)
WO (1) WO1995014680A1 (en)

Families Citing this family (63)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5990136A (en) * 1996-08-21 1999-11-23 Pharmacia & Upjohn Company Isoxazoline derivatives useful as antimicrobials
PT937075E (en) * 1996-11-11 2004-05-31 Altana Pharma Ag NEW IMIDAZO- AND OXAZOLO-PYRIDINES AS PHOSPHODIESTERESE INHIBITORS
WO1998031676A1 (en) * 1997-01-17 1998-07-23 Basf Aktiengesellschaft Process for preparing sulphurous 2-chloro-3-(4,5-dihydroisoxazol-3-yl)-benzoic acids
US6022977A (en) * 1997-03-26 2000-02-08 Dupont Pharmaceuticals Company Dynamic resolution of isoxazoline thioesters to isoxazoline carboxylic acids
CA2315735A1 (en) * 1998-02-13 1999-08-19 Michael R. Barbachyn Substituted aminophenyl isoxazoline derivatives useful as antimicrobials
CA2727762C (en) 1998-05-11 2013-09-10 Basf Aktiengesellschaft Process for synthesizing thioether precursors of herbicides by reaction of anilines with dialkyl disulfides in the presence of an alkyl nitrite
DE19852095A1 (en) 1998-11-12 2000-05-18 Basf Ag Process for the preparation of 2-alkyl-3- (4,5-dihydroisoxazol-3-yl) acylbenzenes
EP1119568B1 (en) * 1998-10-09 2004-02-18 Janssen Pharmaceutica N.V. 4,5-dihydro-isoxazole derivatives and their pharmaceutical use
HU229439B1 (en) 1999-08-21 2013-12-30 Takeda Gmbh Synergistic combination roflumilast and salmeterol
KR100399361B1 (en) 1999-11-04 2003-09-26 주식회사 엘지생명과학 Therapeutic composition comprising caspase inhibitor
CN1137888C (en) * 1999-09-17 2004-02-11 株式会社Lgci Inhibitors of caspases
DE19953024A1 (en) 1999-11-04 2001-05-10 Merck Patent Gmbh Isoxazole derivatives as phosphodiesterase VII inhibitors
JP4202250B2 (en) 2001-07-25 2008-12-24 バイオマリン ファーマシューティカル インコーポレイテッド Compositions and methods for modulating blood brain barrier transport
US7772188B2 (en) 2003-01-28 2010-08-10 Ironwood Pharmaceuticals, Inc. Methods and compositions for the treatment of gastrointestinal disorders
WO2004087211A2 (en) 2003-04-01 2004-10-14 Applied Research Systems Ars Holding N.V. Inhibitors of phosphodiesterases in infertility
KR100594544B1 (en) * 2003-08-27 2006-06-30 주식회사 엘지생명과학 Caspase inhibitors containing isoxazoline ring
CA2537185A1 (en) 2003-08-29 2005-03-10 Ranbaxy Laboratories Limited Inhibitors of phosphodiesterase type-iv
EP1694655A2 (en) * 2003-11-26 2006-08-30 Ranbaxy Laboratories Limited Phosphodiesterase inhibitors
CN101098697B (en) * 2004-03-26 2010-11-10 塞托凯恩药物科学公司 Compound, composition, preparation method and use method related to inhibiting macrophage migration inhibitory factor
PL1768966T3 (en) * 2004-06-17 2012-08-31 Infinity Discovery Inc Coumpounds and methods for inhibiting the interaction of bcl proteins with binding partners
ES2370788T3 (en) * 2005-02-07 2011-12-22 Aerocrine Ab CHECK BREATHED BREATH FLOW DURING ANALYSIS.
CA2601515C (en) * 2005-03-15 2011-02-22 Ganial Immunotherapeutics, Inc. Compounds having immunomodulator activity
CA2789262C (en) 2005-04-28 2016-10-04 Proteus Digital Health, Inc. Pharma-informatics system
AU2006282896A1 (en) 2005-08-26 2007-03-01 Braincells, Inc. Neurogenesis by muscarinic receptor modulation
EP2258357A3 (en) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenesis with acetylcholinesterase inhibitor
EP1928866A1 (en) * 2005-09-05 2008-06-11 Ranbaxy Laboratories Limited Substituted indazoles as inhibitors of phosphodiesterase type-iv
AU2006305620A1 (en) * 2005-10-19 2007-04-26 Ranbaxy Laboratories Limited Compositions of phosphodiesterase type IV inhibitors
WO2007047978A2 (en) 2005-10-21 2007-04-26 Braincells, Inc. Modulation of neurogenesis by pde inhibition
JP2009513672A (en) 2005-10-31 2009-04-02 ブレインセルス,インコーポレイティド GABA receptor-mediated regulation of neurogenesis
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
MX2008014320A (en) 2006-05-09 2009-03-25 Braincells Inc 5 ht receptor mediated neurogenesis.
EP2377531A2 (en) 2006-05-09 2011-10-19 Braincells, Inc. Neurogenesis by modulating angiotensin
US7998971B2 (en) * 2006-09-08 2011-08-16 Braincells Inc. Combinations containing a 4-acylaminopyridine derivative
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
BRPI0717058A2 (en) * 2006-09-22 2013-10-15 Ranbaxy Lab Ltd COMPOUND, PHARMACEUTICAL COMPOSITION, METHOD FOR TREATING, PREVENTING, INHIBITING OR SUPPRESSING AN INFLAMMATORY CONDITION OR DISEASE OR DISEASES OF THE CENTRAL NERVOUS SYSTEM AND METHOD FOR THE PREPARATION OF A COMPOUND
US20100029728A1 (en) * 2006-09-22 2010-02-04 Ranbaxy Laboratories Limited Phosphodiesterase inhibitors
US8795627B2 (en) 2007-03-21 2014-08-05 Raptor Pharmaceuticals Inc. Treatment of liver disorders by administration of RAP conjugates
US8034782B2 (en) 2008-07-16 2011-10-11 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
US8969514B2 (en) 2007-06-04 2015-03-03 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases
WO2008151257A2 (en) 2007-06-04 2008-12-11 Synergy Pharmaceuticals Inc. Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
EP2810951B1 (en) 2008-06-04 2017-03-15 Synergy Pharmaceuticals Inc. Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
ES2919563T3 (en) 2009-02-20 2022-07-27 Enhanx Biopharm Inc Glutathione-based drug delivery system
WO2010099217A1 (en) 2009-02-25 2010-09-02 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
CN110075069A (en) 2009-05-06 2019-08-02 实验室护肤股份有限公司 Include activating agent-calcium phosphate granules compound dermal delivery composition and its application
CN101781294B (en) * 2010-03-10 2012-02-01 天津药物研究院 Imidazole derivative, and preparation method and application thereof
US9616097B2 (en) 2010-09-15 2017-04-11 Synergy Pharmaceuticals, Inc. Formulations of guanylate cyclase C agonists and methods of use
US20120077778A1 (en) 2010-09-29 2012-03-29 Andrea Bourdelais Ladder-Frame Polyether Conjugates
CN107090016A (en) 2011-03-01 2017-08-25 辛纳吉制药公司 The method for preparing guanosine cyclic mono-phosphate activator
UA110241C2 (en) 2011-03-31 2015-12-10 Bayer Ip Gmbh Herbicides and fungicides active phneylisoxazoline 3-5-carboxamide and 3- phneylisoxazoline -5-thioamides
WO2013106547A1 (en) 2012-01-10 2013-07-18 President And Fellows Of Harvard College Beta-cell replication promoting compounds and methods of their use
BR112015006573B1 (en) 2012-09-25 2020-11-03 Bayer Cropscience Ag derivatives of 3-phenylisoxazoline, herbicidal compositions, their uses, and method for controlling undesirable plants
UA113777C2 (en) 2012-09-25 2017-03-10 HERBICIDIC AND FUNGICIDALLY ACTIVE 5-OXYSCOMED 3-PHENYLISOXAZOLINE-5-CARBOXAMIDES AND 5-OXYSAMED 3-PHENYLISOXIDINE-5-OXYZACOLIDINE
US9545446B2 (en) 2013-02-25 2017-01-17 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase and their uses
US9708367B2 (en) 2013-03-15 2017-07-18 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase and their uses
AU2014235209B2 (en) 2013-03-15 2018-06-14 Bausch Health Ireland Limited Guanylate cyclase receptor agonists combined with other drugs
CN105764916B (en) 2013-06-05 2021-05-18 博士医疗爱尔兰有限公司 Ultrapure agonists of guanylate cyclase C, methods of making and using the same
CN114404588A (en) 2013-08-09 2022-04-29 阿德利克斯公司 Compounds and methods for inhibiting phosphate transport
EA039486B1 (en) 2017-06-13 2022-02-01 Байер Акциенгезельшафт Herbicidally active 3-phenylisoxazoline-5-carboxamides of tetrahydro and dihydrofuran carboxylic acids and esters and use thereof
WO2018228986A1 (en) 2017-06-13 2018-12-20 Bayer Aktiengesellschaft Herbicidally active 3-phenylisoxazoline-5-carboxamides of tetrahydro and dihydrofuran carboxamides
ES2984279T3 (en) 2017-08-17 2024-10-29 Bayer Ag 3-phenyl-5-trifluoromethylisoxazoline-5-carboxamides of cyclopentylcarboxylic acids and esters with herbicidal effect
PL3743411T3 (en) 2018-01-25 2023-03-13 Bayer Aktiengesellschaft Herbicidal 3-phenylisoxazolin-5-carboxamides of cyclopentenyl carboxylic acid derivatives
BR112021017924A2 (en) 2019-03-12 2021-11-16 Bayer Ag Herbicidally active 3-phenylisoxazoline-5-carboxamides of cyclopentenyl-carboxylic acid esters containing s
EP3972599B1 (en) 2019-05-21 2025-10-22 Ardelyx, Inc. Combination for lowering serum phosphate in a patient

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4193926A (en) * 1974-03-20 1980-03-18 Schering Aktiengesellschaft 4-(Polyalkoxy phenyl)-2-pyrrolidones
JPS62103070A (en) * 1985-10-29 1987-05-13 Mitsui Toatsu Chem Inc Isoxazoline derivatives and plant growth regulators
US4912120A (en) * 1986-03-14 1990-03-27 Syntex (U.S.A.) Inc. 3,5-substituted 4,5-dihydroisoxazoles as transglutaminase inhibitors
FI875724A7 (en) * 1986-04-29 1987-12-28 Pfizer Calcium-independent cAMP phosphodiesterase inhibitor antidepressant.
IE59813B1 (en) * 1986-05-09 1994-04-06 Warner Lambert Co Styryl pyrazoles, isoxazoles and analogs thereof having activity as 5-lipoxy-genase inhibitors and pharmaceutical compositions containing them
ZA872997B (en) * 1986-05-09 1988-12-28 Warner Lambert Co Novel styryl pyrazoles,isoxazoles and analogs thereof having activity as 5-lipoxygenase inhibitors,pharmaceutical compositions and methods of use therefor
DE3736113A1 (en) * 1987-10-26 1989-05-03 Hoechst Ag DRUGS, PHOSPHORUS-BASED 2-ISOXAZOLINES AND ISOXAZOLES CONTAINING THEREOF, AND METHOD OF PREPARING THESE HETEROCYCLIC COMPOUNDS
US4952700A (en) * 1988-04-25 1990-08-28 W.R. Grace & Co.-Conn. Preparation of isoxazolines and isoxazoles
US4933464A (en) * 1988-04-25 1990-06-12 W. R. Grace & Co.-Conn. Process for forming 3-phenylisoxazolines and 3-phenylisoxazoles
CA2017383A1 (en) * 1989-06-08 1990-12-08 Raymond R. Martodam Use of vanilloids for the treatment of respiratory diseases or disorders
WO1991007177A1 (en) * 1989-11-13 1991-05-30 Pfizer Inc. Pyrimidone derivatives and analogs in the treatment of asthma or certain skin disorders
GB9007762D0 (en) * 1990-04-05 1990-06-06 Beecham Group Plc Novel compounds
EP0451790A1 (en) * 1990-04-12 1991-10-16 Hoechst Aktiengesellschaft 3,5-disubstituted 2-isoxazolines and isoxazoles, process for their preparation, medicines containing them and their use
DE4026018A1 (en) * 1990-08-17 1992-02-20 Hoechst Ag PLANT-PROTECTIVE AGENTS CONTAINING ISOXAZOLINE OR ISOTHIAZOLINE AND NEW ISOXAZOLINE AND ISOTHIAZOLINE
KR930703262A (en) * 1990-11-06 1993-11-29 스튜어트 알. 슈터 Imidazolidinone Compound
PT100441A (en) * 1991-05-02 1993-09-30 Smithkline Beecham Corp PIRROLIDINONES, ITS PREPARATION PROCESS, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM AND USE
AU2869092A (en) * 1991-10-11 1993-05-03 Smithkline Beecham Corporation Heterocyclic 3-phenylpyrrolidin-2-ones, their preparation and use for the manufacture of a medicament for inhibiting tumor necrosis factor production

Also Published As

Publication number Publication date
PT730587E (en) 2000-05-31
EP0730587A1 (en) 1996-09-11
ATE187447T1 (en) 1999-12-15
DK0730587T3 (en) 2000-04-10
EP0730587B1 (en) 1999-12-08
DE69422061D1 (en) 2000-01-13
JP2818820B2 (en) 1998-10-30
DE69422061T2 (en) 2000-03-30
WO1995014680A1 (en) 1995-06-01
JPH09500146A (en) 1997-01-07
GR3032506T3 (en) 2000-05-31
CA2177375A1 (en) 1995-06-01
FI945556A0 (en) 1994-11-25
FI945556A7 (en) 1995-05-27
US5686434A (en) 1997-11-11

Similar Documents

Publication Publication Date Title
ES2139754T3 (en) 3-PHENYL-2-ISOXAZOLINES AS ANTI-INFLAMMATORY AGENTS.
ES2104424T3 (en) ISOXAZOLINE COMPOUNDS AS ANTI-INFLAMMATORY AGENTS.
ES2192192T3 (en) CATECOL DIETS AS SELECTIVE PDE INHIBITORS IV.
ES2154683T3 (en) INDOLES REPLACED AS TYPE IV PHOSPHODIESTERASE INHIBITORS.
CR8254A (en) [1,8] NAFTIDRIN-2-ONAS AND RELATED COMPOUNDS FOR THE TREATMENT OF CHICHOPHRENIA
DK0988292T3 (en) Piperazine derivatives and their use as anti-inflammatory agents
GT200100022A (en) DERIVATIVES OF NICOTINAMIDE BENZOCONDENSADA-HETEROCICLILO USEFUL AS SELECTIVE INHIBITORS OF THE ISOZIMAS PDE4.
MX9405132A (en) TETRAHIDRO PIRAZOLOPIRIDINAS BICICLICAS.
PA8543301A1 (en) DERIVATIVES OF DIHIDRO-BENZO (B) (1,4) DIAZEPIN-2 -ONA AS ANTAGONISTS II MGLUR2
ECSP045476A (en) THIAZOLIDINONES, ITS PREPARATION AND ITS USE AS MEDICATIONS
CR7038A (en) AMIDA DERIVATIVES OF TIAZOLILICO, OXAZOLILICO, PIRROLILICO AND IMIDIAZOLILICO ACIDS USED AS INHIBITORS OF THE ISOZIMAS PDE4
ECSP045228A (en) USEFUL NICOTINAMIDE DERIVATIVES AS PDE4 INHIBITORS
ECSP055676A (en) HETEROCYCLIC PIPERAZINAS REPLACED FOR THE TREATMENT OF CHICHOPHRENIA
PA8446301A1 (en) 2-AMINO-6- (4-PHENOXI-2-SUBSTITUTED) -PIRIDINES SUBSTITUTED
MX9504422A (en) BICYCLE TETRAHYDROPIRAZOLOPYRIDINS.
UY27657A1 (en) USEFUL NICOTINAMIDE DERIVATIVES AS PDE4 INHIBITORS
HN2002000365A (en) LACTAMAS AS TAQUIQUININE ANTAGONISTS
CO5611124A2 (en) BENZOFURAN DERIVATIVES SUBSTITUTED USEFUL IN THE TREATMENT OF HYPER-PROLIFERATIVE DISORDERS
ES2059320T3 (en) NEW DIARYL ALKANOIDS THAT HAVE ACTIVITY AS LIPOXIGENASE INHIBITORS.
BR0212661A (en) Substituted pyrazolyl benzenesulfamide compounds for the treatment of inflammation
HN2000000016A (en) 2-AMINOPIRIDINS CONTAINING SUBSTITUTES OF CONDENSED RING TYPE
ECSP003747A (en) METHOD AND COMPOSITIONS FOR THE TREATMENT OF PULMONARY DISEASES
CL2021001448A1 (en) Crystal forms a, b, d, i of 1–(6–((6–((1r)–1–hydroxyethyl)–8–isopropylamino)pyrido[3,4–d]pyrimidin–2–yl)amino)– 3-pyridyl)piperazin-2-one; pharmaceutical composition comprising them; and its use to treat rheumatoid arthritis, arteriosclerosis, among other diseases (divisional application 201901420).
SV2006002192A (en) AMIDAS OF ACID 5 AND 6-AMINOALQUIL INDOL-2-CARBOXILICO 3-SUBSTITUTES AND RELATED ANALOGS AS INHIBITORS OF CASEINA CINASA IE
MX9603943A (en) ISOXAZOLINE COMPOUNDS AS 5-LIPOOXIGENASE INHIBITORS.

Legal Events

Date Code Title Description
FG2A Definitive protection

Ref document number: 730587

Country of ref document: ES